| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:8621463-8621863 | Common:4; Rare:292 | ||||
| chr16:8674330-8674640 | Common:2; Rare:99; Clinvar:1 | ||||
| chr16:8797541-8797947 | Common:10; Rare:880; Clinvar:19; Clinvar (benign):13; Clinvar (pathogenic):15 | ||||
| chr16:8798018-8798520 | Common:15; Rare:229 | ||||
| chr16:8867594-8867994 | Common:1; Rare:115 | ||||
| chr16:8868289-8868722 | Common:2; Rare:211 | ||||
| chr16:8868920-8869340 | Common:38; Rare:1027 | ||||
| chr16:8962677-8962940 | Common:3; Rare:104 | ||||
| chr16:8963809-8964572 | Common:10; Rare:594 | ||||
| chr16:9091063-9091773 | Common:14; Rare:1359 | ||||
| chr16:9091773-9092272 | Rare:473 | ||||
| chr16:9092405-9092981 | Common:10; Rare:292 | ||||
| chr16:10385760-10386524 | Common:15; Rare:921 | ||||
| chr16:10386471-10387866 | Common:19; Rare:546 | ||||
| chr16:10579877-10580980 | Common:15; Rare:679 |